Canonical Allele Identifier: CA370394220
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16993106G>C , CM000670.2:g.16993106G>C GRCh38
NC_000008.10:g.16850615G>C , CM000670.1:g.16850615G>C GRCh37
NC_000008.9:g.16894986G>C NCBI36
NG_015978.1:g.14060C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000180166.6:c.602C>G MANE Select ENSP00000180166.5:p.Pro201Arg
ENST00000180166.5:c.602C>G ENSP00000180166.5:p.Pro201Arg
ENST00000519941.1:c.306C>G
NM_019851.2:c.602C>G NP_062825.1:p.Pro201Arg
NM_019851.3:c.602C>G MANE Select NP_062825.1:p.Pro201Arg